Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Laboratory for Molecular Medicine, |
RCV000150533 | SCV000197747 | likely benign | not specified | 2014-07-23 | criteria provided, single submitter | clinical testing | Pro97Pro in exon 4 of DSG2: This variant is not expected to have clinical signif icance because it does not alter an amino acid residue and is not located within the splice consensus sequence. Pro97Pro in exon 4 of DSG2 (allele frequency = n/a) |
Labcorp Genetics |
RCV001430314 | SCV001633046 | likely benign | Arrhythmogenic right ventricular dysplasia 10 | 2019-12-19 | criteria provided, single submitter | clinical testing |